Processes for the preparation of 4-alkoxy-3-(acyl or alkyl)oxypicolinamdes

ABSTRACT

A fungicidal 4-methoxy-3-acetyloxypicolinamide may be conveniently prepared in processes that include the coupling together of 4-methoxy-3-acetyloxypicolinic acid or 4-methoxy-3-hydroxypicolinic acid with a key 2-aminopropanoate ester derived from a 1,1-bis(4-fluorophenyl)propane-1,2-diol.

FIELD

The present disclosure concerns processes for the preparation of4-alkoxy-3-(acyl or alkyl)oxypicolinamides. More particularly, thepresent disclosure concerns a process for the preparation of4-methoxy-3-(acetyl or acetyloxymethyl)oxypicolinamides from4-methoxy-3-hydroxypicolinic acids or 4-methoxy-3-acetyloxypicolinicacids.

BACKGROUND

U.S. patent application Ser. Nos. 15/036,314 and 15/036,316 describesinter alia certain heterocyclic aromatic amide compounds of generalFormula

and their use as fungicides. It would be useful to have an efficient andscalable process route to these heterocyclic aromatic amide compoundsfrom inexpensive raw materials.

SUMMARY

The present disclosure concerns processes for the preparation of the4-methoxy-3-(acetyl or acetyloxymethyl)oxypicolinamides of Formula A

wherein Y is CH₃CO or CH₃COOCH₂;from the compounds of Formulas B or D

The compound of Formula A, wherein Y is CH₃CO, may be prepared in aprocess that comprises the following steps:

-   -   a) creating a first mixture containing the compound of Formula        B, an acylating agent or a chlorinating agent, and a base;    -   b) adding the compound of Formula C

-   -   -   wherein X is Cl, Br, HSO₄, H₂PO₄ or CH₃SO₃;            to the first mixture to form a second mixture; and

    -   c) isolating the compound of Formula A from the second mixture,        wherein Y is acetyl (i.e., CH₃CO).

The compound of Formula A, wherein Y is CH₃CO or CH₃COOCH₂, may beprepared in a process that comprises the following steps:

-   -   a) creating a first mixture containing the compound of Formula        D,

-   -   an acylating agent, and a base;    -   b) adding the compound of Formula C

-   -   -   wherein X is Cl, Br, HSO₄, H₂PO₄ or CH₃SO₃;            to the first mixture to form a second mixture;

    -   c) isolating the compound of Formula E from the second mixture;

-   -   -   wherein R¹ is a C₁-C₄ alkyl or CH₂Ph;

    -   d) creating a third mixture containing the compound of Formula        E, an alkali metal base and water;

    -   e) isolating the compound of Formula F from the third mixture;

-   -   f) creating a fourth mixture containing the compound of Formula        F, an acetylating agent or an alkylating agent, and a second        base; and    -   g) isolating the compound of Formula A from the fourth mixture

-   -   -   wherein Y is CH₃CO or CH₃COOCH₂.

The compound of Formula C

-   -   wherein X is Cl, Br, HSO₄, H₂PO₄ or CH₃SO₃;        may be prepared in a process that comprises the following steps:    -   a) creating a first mixture containing the compound of Formula        G,

an acylating agent and a base;

-   -   b) adding the compound of Formula H

to the first mixture to form a second mixture;

-   -   c) isolating the compound of Formula I

from the second mixture;

-   -   d) creating a third mixture containing the compound of Formula        I, an acid and a reducing agent;    -   e) isolating the compound of Formula J from the third mixture;

-   -   f) creating a fourth mixture containing the compound of Formula        J and a strong acid;        -   wherein the strong acid is HCl, HBr, H₂SO₄, H₃PO₄ or            CH₃SO₃H;    -   and    -   g) isolating the compound of Formula C from the fourth mixture.

The compound of Formula C may also be prepared in a process thatcomprises the following steps:

-   -   a) creating a first mixture containing the compound of Formula        H, a reducing agent and an acid;    -   b) isolating the compound of Formula K from the first mixture;

-   -   c) creating a second mixture containing the compound of Formula        G,

an acylating agent and a base;

-   -   d) adding the compound of Formula K to the second mixture to        form a third mixture;    -   e) isolating the compound of Formula L from the third mixture;

-   -   f) creating a fourth mixture containing the compound of Formula        L and a strong acid;        -   wherein the strong acid is HCl, HBr, H₂SO₄, H₃PO₄ or            CH₃SO₃H;    -   and    -   g) isolating the compound of Formula C from the fourth mixture.

Another aspect of the present disclosure are the novel intermediatesproduced in the present process, viz., the compounds:

-   -   wherein R₁ is a C₁-C₄ alkyl or PhCH₂;

-   -   wherein X is Cl, Br, HSO₄, H₂PO₄ or CH₃SO₃; and

DETAILED DESCRIPTION

The term “alkyl” refers to a branched, unbranched, or saturated cycliccarbon chain, including, but not limited to, methyl, ethyl, propyl,butyl, isopropyl, isobutyl, tertiary butyl, pentyl, hexyl, cyclopropyl,cyclobutyl, cyclopentyl, cyclohexyl, and the like.

The term “acyl”, as used herein, refers to an RCO moiety (i.e., RC(O)—)which includes within its scope wherein R is a straight chain orbranched chain alkyl containing from one to six carbon atoms. Specificacyl groups described herein include, for example, CH₃CO (i.e., anacetyl group) and CH₃COOCH₂ (i.e., an acetyloxymethyl group).

The terms “isolate,” “isolating,” or “isolation” as used herein mean topartially or completely remove or separate the desired product from theother components of a finished chemical process mixture using standardmethods such as, but not limited to, filtration, extraction,distillation, crystallization, centrifugation, trituration,liquid-liquid phase separation or other methods known to those ofordinary skill in the art. The isolated product may have a purity thatranges from <50% to >50%, and may be purified to a higher purity levelusing standard purification methods. The isolated product may also beused in a subsequent process step with or without purification.

In the processes described herein the picolinamide of Formula A, whereinY is CH₃CO, may be prepared by coupling 4-methoxy-3-acetyloxypicolinicacid with the 2-aminopropanoate ester portion of the target molecule.Alternatively, picolinamides of Formula A, wherein Y is CH₃CO orCH₃COOCH₂, may be prepared by a process using4-methoxy-3-hydroxypicolinic acid in the described coupling reactionfollowed by addition of the Y group at the end of the process sequence.

-   -   wherein Y is CH₃CO or CH₃COOCH₂.        A. Preparation of Compound of Formula A

The compound of Formula A, wherein Y is CH₃CO, may be prepared directlyfrom the compound of Formula B in the process shown in Scheme I.Picolinic acid B is first activated for coupling by converting it into(a) the corresponding mixed anhydride using an alkyl or benzylchloroformate, or an acid chloride, and a base, or (b) the acid chlorideusing oxalyl chloride or thionyl chloride and a base. The resultingderivative of picolinic acid B, in the form of a mixed anhydride or anacid chloride, can be treated with the amine salt of Formula C, whereinX is Cl, Br, HSO₄, H₂PO₄ or CH₃SO₃, to provide the desired picolinamideof Formula A (Y is CH₃CO). The compound of Formula A may be isolated byemploying standard isolation and purification techniques. Suitablesolvents for this process may include dichloromethane (DCM),1,2-dichloroethane (DCE), isopropyl acetate, tetrahydrofuran (THF),2-MeTHF, and acetonitrile (ACN).

Suitable chloroformate esters (i.e., ClCO₂R) for use in the process mayinclude those wherein R is a C₁-C₄ alkyl or a benzyl. Suitable acidchlorides (i.e., RCOCl) for use in the process may include those whereinR is a C₁-C₄ alkyl. Suitable bases for use in the process may includeone or more of triethylamine (TEA), diisopropylethylamine (DIPEA),pyridine and potassium carbonate. At least 1, at least 2, or at least 3molar equivalents of the base may be used in this process.

In one embodiment, the process shown in Scheme I can be conducted byusing a sulfonating compound in place of the alkyl or benzylchloroformate, or the acid chloride, to prepare the compound of FormulaA. In such a process the compound of Formula B is contacted with thesulfonating compound of Formula B1, wherein R¹ is a C₁-C₄ alkyl and Z isCl or Br, and a base to form the mixed sulfonic-carboxylic anhydride ofFormula B2. Anhydride B2 can then be treated with the amine salt ofFormula C, wherein X is Cl, Br, HSO₄, H₂PO₄ or CH₃SO₃, or the amine ofFormula J to provide the desired picolinamide of Formula A (Y is CH₃CO).

The compound of Formula A may also be prepared from the compound ofFormula D in the process shown in Scheme II. Picolinic acid D is firstconverted into the compound of Formula D1, which is not isolated, usingat least about 2 equivalents of an alkyl or benzyl chloroformate of theFormula ClCO₂R, wherein R is a C₁-C₄ alkyl or a benzyl, and at leastabout 3 equivalents of a base. The reaction mixture containing compoundD1 may then be combined with the compound of Formula C to producepicolinamide E. Suitable bases such as, for example, TEA, DIPEA orsimilar trialkylamine bases, may be used in these reactions. Treatmentof Compound E with an alkali metal base, such as LiOH, NaOH, KOH, ormixtures thereof, in the presence of water and, optionally a co-solvent,such as, for example, tetrahydrofuran (THF), 2-tetrahydrofuran(2-MeTHF), DME, dioxane, ACN or a C₁-C₄ alcohol, may provide thecompound of Formula F. Acetylation of Compound F with acetic anhydride,acetyl chloride or other acetylating agents commonly used in the art andwith the use of a base, or using Schotten-Baumann reaction conditions,may provide the compound of Formula A wherein Y is CH₃CO. Alkylation ofCompound F with CH₃COOCH₂Br and a base may provide the compound ofFormula A wherein Y is CH₃COOCH₂. Bases useful in these reactions may beselected from at least one of pyridine, TEA, and DIPEA. The

compounds of Formulas A, E and F may be isolated by employing standardisolation and purification techniques.

In the hydrolysis reaction that converts compound E to compound F inScheme II, the compound of Formula E1 under certain conditions may beisolated as an intermediate in that reaction.

In some embodiments, the picolinamide of Formula A, wherein Y is CH₃COor CH₃COOCH₂, may be prepared by a process using the amine of Formula Jin place of the amine salt of Formula C.

B. Preparation of the Compound of Formula C

The compound of Formula C may be prepared by two different processeswith both starting from the diol compound of Formula H. In the first ofthe two processes, shown in Scheme III, the diol compound H may becoupled with the BOC-L-alanine compound G to produce the compound ofFormula I. The coupling reaction may be conducted by utilizing the mixedanhydride derivative of compound G, which may be prepared by treating Gwith an acid chloride of formula RCOCl, wherein R is a C₁-C₄ alkyl, abase and DMAP (4-(dimethylamino)pyridine). Suitable solvents for thisreaction may include one or more of DCM, DCE, THF, 2-MeTHF and ACN andsuitable bases may include one or more of TEA, DIPEA, and pyridine.

In the second step of the process shown in Scheme III, the tertiaryhydroxyl group and the BOC group in the compound of Formula I areremoved by use of a reducing agent combined with an acid. Suitablereducing agents for this transformation may include borohydride reagentssuch as, but not limited to, sodium borohydride and sodiumtriacetoxyborohydride, and organosilicon hydrides such as, for example,triethylsilane, poly(methylhydrosiloxane) (PMHS) and1,1,3,3-tetramethyldisiloxane (TMDS). Suitable acids for use with thereducing agents may include, but are not limited to, trifluoroaceticacid and methanesulfonic acid. Finally, compound J may be converted intothe amine salt compound of Formula C by treatment with strong acid HXutilizing anhydrous conditions, wherein HX may be selected from HCl,HBr, H₂SO₄, H₃PO₄ or CH₃SO₃H.

The second process for the preparation of the compound of Formula C isshown in Scheme IV. The diol compound of Formula H may be treated withan acid and a reducing agent to produce the alcohol of Formula K.Suitable reducing agents for this transformation include organosiliconhydrides such as, for example, triethylsilane, poly(methylhydrosiloxane)(PMHS) and 1,1,3,3-tetramethyldisiloxane (TMDS), and borohydridereagents such as, but not limited to, sodium borohydride and sodiumtriacetoxyborohydride. Suitable acids for use with the reducing agentsmay include, but are not limited to, trifluoroacetic acid andmethanesulfonic acid. The alcohol of Formula K may then be coupled withthe BOC-L-alanine compound of Formula G to produce the compound ofFormula L using the reagents and conditions described herein for thepreparation of the compound of Formula I in Scheme III. Finally,compound L may be converted into the amine salt compound of Formula C bytreatment with strong acid HX

utilizing anhydrous conditions, wherein HX may be selected from HCl,HBr, H₂SO₄, H₃PO₄ or CH₃SO₃H.C. Preparation of Compound of Formula H

The diol of Formula H may be prepared from (4-fluorophenyl)magnesiumbromide and (S)-ethyl lactate as described herein. A solution of aboutthree molar equivalents of (4-fluorophenyl)magnesium bromide in THF canbe treated at about 0° C. with (S)-ethyl lactate. The diol of Formula Hmay be recovered by employing standard isolation and purificationtechniques.

Chemical literature describing the preparation of(S)-(1,1-bis-aryl)propane-1,2-diols like the compound of Formula Hinclude: (1) Eur. J. Org. Chem. 2005, 1082, (2) Tetrahedron Lett. 1989,30, 3659, (3) Tetrahedron: Asymmetry, 1990, 1, 199, and (4) U.S. Pat.No. 4,628,120. For related transformations involving aryl Grignardaddition to (S)-isopropyl lactate, for the synthesis of(S)-(1,1-bisaryl)propane-1,2-diols, see J. Am. Chem. Soc. 1990, 112,3949.

D. Preparation of Compound of Formula B

The conversion of the 4-methoxy-3-hydroxypicolinic acid to the 3-acetoxycompound of Formula B, may be accomplished by acetylating the compoundof Formula D with one or more acetylation reagents selected from aceticanhydride and acetyl chloride, bases selected from pyridine, alkylsubstituted pyridines, and trialkylamines, or utilization ofSchotten-Baumann reaction conditions.

The product obtained by any of these processes, can be recovered byconventional means, such as evaporation, filtration or extraction, andcan be purified by standard procedures, such as by recrystallization orchromatography.

The following examples are presented to illustrate the disclosure.

EXAMPLES Example 1a. (S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-acetoxy-4-methoxypicolinamido)propanoate

A 100 mL flask equipped with a stir bar was charged with3-acetoxy-4-methoxypicolinic acid (427 mg, 2 mmol) and DCM (10 mL). Thesuspension was cooled to −5° C. Triethylamine (445 mg, 4.4 mmol) wasadded in one portion, followed by addition of ethyl carbonochloridate(0.19 mL, 2 mmol) slowly via syringe. After 10 minutes, a solution of(S,S)-1,1-bis(4-fluorophenyl)propan-2-yl 2-aminopropanoate hydrochloride(712 mg, 2 mmol) in DCM (2 mL) was added. After the reaction appearedcomplete by HPLC, 20% aqueous K₂CO₃ solution (10 mL) was charged, andthe mixture was stirred vigorously for 30 min at rt. The organic layerwas separated. The aqueous layer was extracted with DCM. The combinedorganic layers were washed with water, 1N HCl and water. The separatedorganic layer was concentrated to provide a light yellow foam (1.5 g,98%): ¹H NMR (400 MHz, CDCl₃) δ 8.39 (s, 1H), 8.32 (d, J=5.4 Hz, 1H),7.26-7.16 (m, 4H), 7.03-6.87 (m, 5H), 5.71 (dq, J=9.6, 6.1 Hz, 1H), 4.55(dd, J=8.0, 7.1 Hz, 1H), 4.04 (d, J=9.6 Hz, 1H), 3.91 (s, 3H), 2.38 (s,3H), 1.22 (d, J=6.1 Hz, 3H), 0.99 (d, J=7.2 Hz, 3H); ¹⁹F NMR (376 MHz,CDCl₃) δ −115.61, −115.96; HRMS-ESI (m/z) [M+H]+ calcd for C₂₇H₂₇F₂N₂O₆,512.1759; found, 513.1825.

Example 1b. (S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-acetoxy-4-methoxypicolinamido)propanoate

Dichloromethane (64.6 L) and 3-acetoxy-4-methoxypicolinic acid (6.82 kg)were charged to a stainless steel reactor with stirring under nitrogenatmosphere at 25-30° C. The solution was cooled to −15° C., andN,N-diisopropylethylamine (9.2 kg, 2.2 eq) was added dropwise andstirred for 5 min. Ethyl chloroformate (3.68 kg, 1.05 eq) was addeddropwise and stirred for 30 min. Finally, a solution of 11.5 kg of(S,S)-1,1-bis(4-fluorophenyl)propan-2-yl 2-aminopropanoate hydrochloridein 32.2 L dichloromethane added dropwise and stirred at −15° C. for 30min. The reaction mixture was warmed to 0-2° C., and saturated aqueoussodium bicarbonate solution (57.5 L, 5.75 kg of NaHCO3 in 57.5 L water)was added and stirred for 10-15 min. The aqueous layer was separated andextracted with dichloromethane (1×57.5 L). Combined the organic layers,washed with water (1×57.5 L), then with mixture of 1N HCl and brinesolution (1×64.4 L, 32.2 L 1N HCl and 32.2 L brine). Organic layer wasdried with sodium sulphate (11.5 kg), filtered, washed withdichloromethane (23.0 L) and concentrated below 40° C. under vacuum(500-600 mm Hg) until no distillate was observed. Added isopropylalcohol (23.0 L) and concentrated below 45° C. under vacuum (500-600 mmHg) to give a thick syrup. Isopropyl alcohol (11.5 L) and n-heptane(11.5 L) were charged, heated to 50-55° C. and stirred at 50-55° C. for30 min. The solution was cooled to 25-30° C., n-heptane (11.5 L) wasadded, and the solution was stirred at 25-30° C. for 5 h. Additionaln-heptane (34.5 L) was added, the solution was stirred at 25-30° C. for6 h. The resulting solid was filtered, washed with n-heptane (57.5 L)and dried at 35-40° C. under vacuum (500-600 mm Hg) to give(S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-acetoxy-4-methoxypicolinamido)propanoate as an off-white powder(14.74 kg, 89.0% yield). HPLC (Zorbax SB-Phenyl, (250×4.6) mm, 5.0 μm;0.1% Formic acid in 50:50 water:ACN, Flow rate: 1.0 mL/min) showed theproduct to be 98.3% pure.

Example 1c. (S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-acetoxy-4-methoxypicolinamido)propanoate

A 500 mL flask equipped with magnetic stir bar and nitrogen inlet wascharged with 3-acetoxy-4-methoxypicolinic acid (11.5 g, 54.5 mmol), DCM(140 ml), pyridine (4.84 ml, 59.9 mmol) & 1 drop of DMF. The flask wascooled to 0° C., and oxalyl chloride (4.77 ml, 54.5 mmol) was slowlyadded via syringe. The resulting dark solution was allowed to stir forapproximately 15 min. The solution was then added via cannula to a cold(0° C.) suspension of (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl2-aminopropanoate hydrochloride (19.38 g, 54.5 mmol) and triethylamine(15.94 ml, 114 mmol) in DCM (70 ml) in a 1 L flask. When the additionwas complete, the bath was removed, and the solution was allowed to warmto rt. Upon completion of the reaction as judged by LCMS, the reactionmixture was poured into saturated aqueous NH₄Cl solution (200 mL) andtransferred to a separatory funnel. The organic layer was separated, andthe aqueous layer was extracted with CH₂Cl₂ (1×200 mL). The combinedorganic layers were dried with Na₂SO₄, filtered and concentrated toafford a tan foam/black oil. The crude material was purified via silicagel chromatography (0-100% gradient ethyl acetate in hexanes) to affordthe title compound as a pink solid foam (14 g, 50.2%, 90% purity):spectroscopic data identical to that listed above.

Example 1d. (S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-acetoxy-4-methoxypicolinamido)propanoate

A 100 mL flask equipped with magnetic stir bar and nitrogen inlet wascharged with 3-acetoxy-4-methoxypicolinic acid (1.00 g, 4.74 mmol), DCM(23.7 ml), and triethylamine (0.661 ml, 4.74 mmol). The flask was cooledto 0° C., and pivaloyl chloride (0.583 ml, 4.74 mmol) was slowly addedto the reaction mixture. The reaction mixture was allowed to stir for 15min at 0° C. (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl 2-aminopropanoatehydrochloride (1.685 g, 4.74 mmol) was then added in one portion. Thereaction mixture was poured into saturated aqueous NH₄Cl solution andtransferred to a separatory funnel. The organic layer was separated,washed with saturated aqueous NaHCO₃ solution, then brine and then driedwith Na₂SO₄. The solution was filtered and concentrated to afford a anoff-white foam. The crude material was purified via silica gelchromatography (0-100% gradient ethyl acetate in hexanes) to afford thetitle compound as a white foam (1.7 g, 59.5%, 90% purity): spectroscopicdata identical to that listed above.

Example 1e. (S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-((ethoxycarbonyl)oxy)-4-methoxypicolinamido)propanoate

A 250 mL flask equipped with a stir bar was charged with3-hydroxy-4-methoxypicolinic acid (0.846 g, 5 mmol) and backfilled withnitrogen. DCM (25 mL) was added to the reaction flask and the resultingwhite heterogeneous mixture was cooled to 0° C. Triethylamine (2.3 mL,16.5 mmol) was added and the reaction mixture became a homogeneouscolorless solution over the course of ten minutes of vigorous stirring.Ethyl chloroformate (1.0 mL, 10.5 mmol) was slowly added to the reactionmixture and a white precipitate began to form. After stirring for 15 minat 0° C., (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl 2-aminopropanoatehydrochloride (1.78 g, 5.00 mmol) was added to the flask in one portion.The reaction mixture was stirred at 0° C. for 3 min, at which time thereaction was quenched with 20 mL of water and 5 mL of 2N HCl. Thebiphasic mixture was diluted with DCM and transferred to a separatoryfunnel. The layers were separated and the organic layer was dried withNa₂SO₄, filtered and concentrated to afford a pale yellow oil. The crudematerial was purified via silica gel chromatography by eluting with anethyl acetate/hexane gradient to afford the title compound as a whitesolid (2.3 g, 85%): mp 48-64° C.; ¹H NMR (400 MHz, CDCl₃) δ 8.45-8.25(m, 2H), 7.38-7.12 (m, 4H), 7.09-6.85 (m, 5H), 5.71 (dq, J=9.7, 6.2 Hz,1H), 4.67-4.54 (m, 1H), 4.34 (q, J=7.1 Hz, 2H), 4.04 (d, J=9.6 Hz, 1H),3.92 (s, 3H), 1.40 (t, J=7.1 Hz, 3H), 1.22 (d, J=6.2 Hz, 3H), 0.99 (d,J=7.2 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 172.1, 162.2, 161.7 (d,J=246.0 Hz), 161.6 (d, J=245.6 Hz), 159.4, 152.5, 146.8, 141.7, 137.7,136.9, 136.8, 129.6 (d, J=7.8 Hz), 129.5 (d, J=7.8 Hz), 115.7 (d, J=21.4Hz), 115.4 (d, J=21.2 Hz), 110.0, 73.1, 65.4, 56.3, 56.1, 47.8, 19.1,18.1, 14.1; ¹⁹F NMR (471 MHz, CDCl3) δ −115.59, −115.95; HRMS-ESI (m/z)[M+H]+ calcd for C₂₈H₂₉F₂N₂O₇, 543.1937; found, 543.1932.

Example 1f. (S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-((isobutoxycarbonyl)oxy)-4-methoxypicolinamido)propanoate

A 250 mL flask equipped with a stir bar was charged with3-hydroxy-4-methoxypicolinic acid (0.846 g, 5 mmol) and backfilled withnitrogen. DCM (25 mL) was added to the reaction flask and the resultingwhite heterogeneous mixture was cooled to 0° C. Triethylamine (2.3 mL,16.5 mmol) was added and the reaction mixture became a homogeneouscolorless solution over the course of ten minutes of vigorous stirring.Isobutyl chloroformate (1.4 mL, 10.5 mmol) was slowly added to thereaction mixture and a white precipitate began to form. After stirringfor 15 min at 0° C., (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl2-aminopropanoate hydrochloride (1.78 g, 5.00 mmol) was added to theflask in one portion. The reaction mixture was stirred at 0° C. for 3min, at which time the reaction was quenched with 20 mL of water and 5mL of 2N HCl. The biphasic mixture was diluted with DCM and transferredto a separatory funnel. The layers were separated and the organic layerwas dried with Na₂SO₄, filtered and concentrated to afford a pale yellowoil. The crude material was purified via silica gel chromatography byeluting with an ethyl acetate/hexane gradient to afford the titlecompound as a white solid (2.3 g, 81%): mp 47-63° C.; ¹H NMR (400 MHz,CDCl₃) δ 8.38-8.26 (m, 2H), 7.26-7.18 (m, 4H), 7.04-6.88 (m, 5H), 5.71(dq, J=9.6, 6.2 Hz, 1H), 4.66-4.51 (m, 1H), 4.07 (d, J=6.7 Hz, 2H), 4.04(d, J=10.0 Hz, 1H), 3.92 (s, 3H), 2.19-1.98 (m, 1H), 1.22 (d, J=6.1 Hz,3H), 0.99 (d, J=6.7 Hz, 6H), 0.99 (d, J=7.2 Hz, 3H); ¹³C NMR (101 MHz,CDCl₃) δ 172.2, 162.2, 161.73 (d, J=246.0 Hz), 161.65 (d, J=245.6 Hz),159.4, 152.6, 146.8, 141.7, 137.8, 136.9, 136.9, 129.61 (d, J=7.8 Hz),129.54 (d, J=8.0 Hz), 115.68 (d, J=21.3 Hz), 115.39 (d, J=21.3 Hz),109.9, 75.3, 73.1, 56.3, 56.1, 47.8, 27.8, 19.1, 18.9, 18.1; ¹⁹F NMR(471 MHz, CDCl₃) δ −115.59, −115.95; HRMS-ESI (m/z) [M+H]+ calcd forC₃₀H₃₃F₂N₂O₇, 571.2250; found, 571.2253.

Example 1g. (S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-hydroxy-4-methoxypicolinamido)propanoate

A vial equipped with a stir bar was charged with(S,S)-1,1-bis(4-fluorophenyl)propan-2-yl2-(3-((ethoxycarbonyl)oxy)-4-methoxypicolinamido)propanoate (543 mg, 1mmol, employed as an 8:1 mixture of the title starting material toproduct: (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl2-(3-hydroxy-4-methoxypicolinamido)propanoate) and THF (5 mL). Lithiumhydroxide hydrate (71 mg, 1.69 mmol) was placed in a separate vial,dissolved in water (2.5 mL) and added to the reaction flask. Thereaction immediately turned from clear colorless to yellow. The reactionwas allowed to stir for 3 h at RT. The reaction was acidified to pH of 2with 2N HCl (0.8 mL) and diluted with 25 mL of ethyl acetate. Theorganic layer was concentrated to give a yellow oil. The crude materialwas purified via silica gel chromatography by eluting with an ethylacetate/hexane gradient to afford the title compound as a white foam(397 mg, 84%): ¹H NMR (400 MHz, CDCl₃) δ 12.06 (s, 1H), 8.32 (dd, J=6.7,4.3 Hz, 1H), 7.98 (d, J=5.2 Hz, 1H), 7.32-7.14 (m, 4H), 7.03-6.89 (m,4H), 6.87 (d, J=5.2 Hz, 1H), 5.73 (dq, J=9.8, 6.2 Hz, 1H), 4.61-4.47 (m,1H), 4.05 (d, J=9.8 Hz, 1H), 3.94 (s, 3H), 1.25 (d, J=6.1 Hz, 3H), 1.07(d, J=7.2 Hz, 3H); 13C NMR (101 MHz, CDCl3) δ 171.6, 168.6, 161.8 (d,J=246.1 Hz), 161.7 (d, J=245.7 Hz), 155.4, 148.8, 140.4, 136.8 (d, J=3.4Hz), 136.7 (d, J=3.4 Hz), 130.4, 129.5 (d, J=7.8 Hz), 129.5 (d, J=7.8Hz), 115.7 (d, J=21.3 Hz), 115.4 (d, J=21.3 Hz), 109.5, 73.3, 56.1,56.1, 47.9, 19.1, 17.7; ¹⁹F NMR (471 MHz, CDCl₃) δ −115.46, −115.80;HRMS-ESI (m/z) [M+H]+ calcd for C₂₅H25F2N2O5, 471.1726; found, 471.1724.

Example 1h. (S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-acetoxy-4-methoxypicolinamido)propanoate

A 2 L flask equipped with a stir bar was charged with(S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-hydroxy-4-methoxypicolinamido)propanoate (25 g, 51.0 mmol),pyridine (250 mL) and acetic anhydride (250 mL, 2.65 mol). The reactionwas stirred for 1 h at RT and then the solvents were removed undervacuum. Heptane was added and the mixture was concentrated. This stepwas repeated to ensure complete azeotropic removal of any residualsolvent. Dichloromethane and sat. aqueous ammonium chloride were addedto the residue and the layers were separated. The aqueous layer wasextracted with dichloromethane (1×) and the combined organic layers weredried over Na₂SO₄, filtered and concentrated under vacuum to yield anoff-white foam. The crude material was purified via silica gelchromatography by eluting with an ethyl acetate/hexane gradient toafford the title compound as a white foam (25.1 g, 95%, 99% purity): ¹HNMR (500 MHz, CDCl₃) δ 8.39 (s, br, 1H), 8.32 (d, J=5.4 Hz, 1H),7.26-7.19 (m, 4H), 7.04-6.88 (m, 5H), 5.71 (dq, J=9.6, 6.1 Hz, 1H),4.62-4.49 (m, 1H), 4.04 (d, J=9.6 Hz, 1H), 3.90 (s, 3H), 2.38 (s, 3H),1.22 (d, J=6.2 Hz, 3H), 0.99 (d, J=7.1 Hz, 3H); 13C NMR (126 MHz, CDCl3)δ 172.2, 170.3, 162.9, 161.7 (d, J=246.1 Hz), 161.6 (d, J=245.6 Hz),160.3, 145.7, 144.0, 142.4, 136.9 (d, J=3.3 Hz), 136.8 (d, J=3.4 Hz),129.6 (d, J=5.9 Hz), 129.5 (d, J=5.8 Hz), 115.7 (d, J=21.3 Hz), 115.4(d, J=21.1 Hz), 109.6, 73.0, 56.2, 56.1, 48.0, 20.9, 19.2, 17.8; ¹⁹F NMR(471 MHz, CDCl₃) δ −115.60, −115.96; HRMS-ESI (m/z) [M+H]+ calcd forC₂₇H27F2N2O6, 513.1832; found, 513.1849.

Example 1i. (S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-acetoxymethoxy-4-methoxypicolinamido)propanoate

A three-neck 500 mL flask equipped with a stirbar, reflux condenser,thermocouple and nitrogen inlet was charged with(S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-hydroxy-4-methoxypicolinamido)propanoate (4.9 g, 10.42 mmol)) andacetone (104 ml). Solid potassium carbonate (2.88 g, 20.83 mmol) wasadded, followed by the addition of bromomethyl acetate (1.532 ml, 15.62mmol). A catalytic amount of NaI was added, and the mixture was heatedto 50° C. for three hours. The mixture was cooled, filtered andconcentrated. The crude material was purified via silica gelchromatography by eluting with an ethyl acetate/hexane gradient toafford the title compound as a white foam (3.9 g, 69%): ¹H NMR (400 MHz,CDCl₃) δ 8.26 (d, J=5.4 Hz, 1H), 8.20 (d, J=7.8 Hz, 1H), 7.28-7.18 (m,4H), 7.02-6.91 (m, 5H), 5.76-5.70 (m, 1H), 5.72 (s, 2H), 4.56 (9, J=7.3Hz, 1H), 4.05 (d, J=9.7 Hz, 1H), 3.91 (s, 3H), 2.06 (s, 3H), 1.24 (d,J=6.1 Hz, 3H), 1.00 (d, J=7.2 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 172.2,170.3, 162.9, 161.7 (d, J=246.0 Hz), 161.6 (d, J=245.5 Hz), 160.3,145.7, 144.0, 142.3, 136.9 (d, J=3.3 Hz), 136.8 (d, J=3.3 Hz), 129.6 (d,J=7.8 Hz), 129.5 (d, J=7.9 Hz), 115.7 (d, J=21.4 Hz), 115.4 (d, J=21.3Hz), 109.6, 89.5, 73.0, 56.2, 56.1, 48.1, 20.8, 19.1, 17.8; ¹⁹F NMR (376MHz, CDCl₃) δ −115.59, −115.97; HRMS-ESI (m/z) [M+H]⁺ calcd forC₂₈H₂₉F₂N₂O₇, 543.1937; found, 543.1948.

Example 1j. (S,S)-1,1-bis(4-fluorophenyl)-1-hydroxypropan-2-yl2-((tert-butoxycarbonyl)amino)propanoate

A 250 mL flask equipped with a stir bar was charged with(S)-2-[(tert-butoxycarbonyl)amino]propanoic acid (5.68 g, 30.0 mmol) andDCM (125 ml) and cooled to 0° C. Triethylamine (8.72 mL, 62.5 mmol) wasadded to the reaction flask. As pivaloyl chloride (3.69 ml, 30.0 mmol)was slowly added to the reaction mixture a white precipitate began toform. After stirring for 15 min at 0° C.,(S)-1,1-bis(4-fluorophenyl)propane-1,2-diol (6.61 g, 25 mmol) was added,followed by N,N-dimethylpyridin-4-amine (0.153 g, 1.250 mmol) which ledto an exotherm up to 4.4° C. After the additions, the reaction wasstirred for 2 h at RT. The reaction was quenched with water, and thelayers were separated. The aqueous layer was extracted once with DCM.The combined organic layers were dried with Na₂SO₄, filtered andconcentrated to afford an oil. The crude material was purified viasilica gel chromatography by eluting with an ethyl acetate/hexanegradient to afford the title compound as a white solid (8.75 g, 80%): mp50-60° C.; ¹H NMR (400 MHz, CDCl₃) δ 7.50-7.42 (m, 2H), 7.42-7.36 (m,2H), 7.03-6.94 (m, 4H), 5.91 (q, J=6.2 Hz, 1H), 4.96 (d, J=7.8 Hz, 1H),4.20-4.10 (m, 1H), 3.02-2.73 (m, 1H), 1.41 (s, 8H), 1.18 (d, J=6.3 Hz,3H), 0.92 (d, J=7.2 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 172.4, 161.9 (d,J=246.7 Hz), 161.9 (d, J=246.7 Hz), 155.0, 140.7 (d, J=3.3 Hz), 138.6(d, J=2.8 Hz), 127.5 (d, J=8.0 Hz), 127.4 (d, J=8.2 Hz), 115.2 (d,J=21.6 Hz), 80.0, 79.0, 74.9, 49.2, 28.3, 18.0, 14.4 (one peak ismissing due to incidental equivalence); ¹⁹F NMR (376 MHz, CDCl₃) δ−115.21, −115.25; HRMS-ESI (m/z) [M+Na]+ calcd for C₂₃H27F2NNaO5,458.1750; found, 458.1760.

Example 1k. (S,S)-1,1-bis(4-fluorophenyl)-1-hydroxypropan-2-yl2-((tert-butoxycarbonyl)amino)propanoate

Anhydrous THF (49.4 L, 7.6 volume) and Boc-L-alanine (6.3 kg, 1.35 eq)were charged into a stainless steel reactor with stirring under nitrogenatmosphere at 25-30° C. The reaction mixture was cooled to 0-3° C., andtriethylamine (9.7 L, 2.8 eq) was added dropwise at 0-3° C. and stirredfor 5 min. Pivaloyl chloride (4.0 Kg, 1.35 eq) was added dropwise at0-3° C. and stirred at 0-3° C. for 1 h. 4-(Dimethylamino)pyridine (0.15kg, 0.05 eq) was added in one portion and stirred for 5 min. Finally, asolution of (S)-1,1-bis(4-fluorophenyl)propane-1,2-diol in THF (6.5 kg,1.0 eq in 19.5 L of THF) was added dropwise at 0-3° C. The reactionmixture was stirred at 25-30° C. for 3 h. The reaction mixture wasconcentrated below 40° C. under vacuum (500-600 mm Hg) until nodistillate was observed. Ethyl acetate (49.4 L) and water (24.7 L) wereadded and stirred for 10 min. The layers were separated. The organiclayer was washed with saturated ammonium chloride solution (1×24.7 L),then with saturated sodium bicarbonate solution (1×24.7 L) and brinesolution (1×13.0 L,). The organic layer was dried with sodium sulphate(3.25 kg), filtered, washed with ethyl acetate (6.5 L) and concentratedcompletely below 40° C. under vacuum (500-600 mm Hg) until no distillatewas observed. Added hexanes (10.4 L) and concentrated below 40° C. undervacuum (500-600 mm Hg) to give a thick syrup. Hexanes (13.0 L) wereadded and stirred at 25-30° C. for 10 min. The solution was seeded withauthentic product (13.0 g) and stirred at 25-30° C. for 12 h. The solidwas filtered, washed with hexanes (2×6.5 L, 2.0 volume) and dried at38-42° C. under vacuum (500-600 mm Hg) to give(S,S)-1,1-bis(4-fluorophenyl)-1-hydroxypropan-2-yl2-((tert-butoxycarbonyl)amino)propanoate as off white solid (8.4 kg,78.4% yield). HPLC (Hypersil BDS C18, (250×4.6) mm, 5.0 am; A: 0.1% TFAin water, B: ACN, Flow: 1.0 mL/min) showed the product to be 94.0% pure.

Example 1l. (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl 2-aminopropanoatehydrochloride

A 3 neck flask equipped with a stir bar, temperature probe and nitrogeninlet was charged with trifluoroacetic acid (8.85 ml, 115 mmol) andcooled to 0° C. Sodium borohydride (0.434 g, 11.5 mmol) was slowlyadded, followed by slow addition of(S,S)-1,1-bis(4-fluorophenyl)-1-hydroxypropan-2-yl2-((tert-butoxycarbonyl)amino)propanoate (1 g, 2.3 mmol) in DCM (2.3mL). The reaction mixture was stirred at 0° C. for 1 h and then at RTfor 3 h. The reaction mixture was quenched with 2M NaOH to pH>12, anddiluted with DCM. The organic layer was washed with brine. The combinedaqueous layers were extracted once with DCM. The combined organic layerswere concentrated to give an oil. The crude free base of the amine wastreated with 2 mL of 4M HCl in dioxane and then concentrated to give apink gummy oil. MTBE (2 mL) was added and a white precipitate began toform. The heterogeneous mixture was stirred for 30 min at 0° C. Vacuumfiltration of the hetereogenous mixture afforded the title compound as awhite solid (355 mg, 40%): ¹H NMR (300 MHz, DMSO-d6) δ 8.38 (s, 3H),7.56-7.40 (m, 4H), 7.18-7.10 (m, 4H), 5.77 (dq, J=12.2, 6.2 Hz, 1H),4.27 (d, J=10.1 Hz, 1H), 3.91 (q, J=7.1 Hz, 1H), 1.17 (d, J=6.1 Hz, 3H),0.81 (d, J=7.2 Hz, 3H); ¹³C NMR (101 MHz, DMSO-d6) δ 169.5, 161.0 (d,J=243.2 Hz), 160.9 (d, J=242.7 Hz), 137.8 (d, J=3.2 Hz), 137.3 (d, J=3.2Hz), 130.0 (d, J=7.9 Hz), 129.8 (d, J=7.9 Hz), 115.4 (d, J=21.1 Hz),115.2 (d, J=21.0 Hz), 73.7, 54.7, 47.6, 18.8, 15.0; ¹⁹F NMR (376 MHz,DMSO-d6) δ −115.89, −116.29; ESIMS m/z 320.1 ([M+H]+).

Example 1m. (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl 2-aminopropanoatehydrochloride

A 3 neck flask equipped with a stir bar, temperature probe and nitrogeninlet was charged with sodium triacetoxyborohydride (4.24 g, 20 mmol)and trifluoroacetic acid (15.4 ml, 200 mmol) at 0° C. After 10-15minutes at 0-5° C., (S,S)-1,1-bis(4-fluorophenyl)-1-hydroxypropan-2-yl2-((tert-butoxycarbonyl)amino)propanoate (4.35 g, 10 mmol) in DCM (5 mL)was added. The reaction mixture was stirred at rt for 4-5 h. Thereaction mixture was concentrated and rediluted with DCM. The organiclayer was washed with aqueous 20% K₂CO₃ solution. The aqueous layer wasextracted with additional DCM. The combined organic layers were washedwith water. The organic layer was concentrated to give an oil. The crudefree base of the amine was diluted with MTBE then treated with 4M HCl indioxane (3.0 mL). The white precipitate began to form. The heterogeneousmixture was stirred for 0.5-1 hour at RT. Vacuum filtration of the solidproduct afforded the title compound as a white solid (2.7 g, 75%):spectroscopic data were identical to the compound isolated in Example1l.

Example 1n. (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl 2-aminopropanoatehydrochloride

Trifluoroacetic acid (170.3 L) was charged in to a glass-lined reactorwith stirring under nitrogen atmosphere at 25-30° C. and cooled to 0-2°C. Sodium triacetoxyborohydride (29.7 kg, 2.7 eq) was added in portions(4 lots in every 5 min interval) at 0-10° C. and stirred at 13-17° C.for 30 min. A solution of(S,S)-1,1-bis(4-fluorophenyl)-1-hydroxypropan-2-yl-2-((tert-butoxycarbonyl)amino)propanoate in dichloromethane (22.7 kg, 1.0 equiv., in 22.7 L ofdichloromethane) was added dropwise by maintaining the temperature at8-10° C. and stirred at 13-17° C. for 2 h. After completion of thereaction, the reaction mixture was concentrated below 50° C. undervacuum (500-600 mm Hg), then the mass was co-evaporated with toluene(2×90.8 L) to give a pale yellow syrup which was dissolved indichloromethane (227 L). 15% Aqueous ammonium chloride solution (794.5L,) was added slowly to the above mass at 25-30° C. and stirred at25-30° C. for 15 min. The layers were separated. The aqueous layer wasextracted with dichloromethane (2×113.5 L) The combined organic extractswere washed with brine (1×113.5 L), dried with sodium sulphate (22.7 kg)and filtered. The filtrate was concentrated below 35° C. under vacuum(500-600 mm Hg) to give a pale brown syrup. MTBE (68.1 L) and n-heptane(22.7 L,) were added to the syrup and cooled to 8-12° C. 4N HCl indioxane (20.45 L) was added at 8-12° C. and stirred for 30 min at 25-30°C. Added n-heptane (113.5 L) and stirred at 25-30° C. for 30 min. Theresulting solid was filtered under nitrogen and washed with n-heptane(68.1 L) to give a first crop.

The filtrate was concentrated below 50° C. under vacuum (500-600 mm Hg).MTBE (45.4 L) and 4N HCl in dioxane (11.4 L) were added and stirred at25-30° C. for 1 h. The solution was concentrated below 50° C. undervacuum (500-600 mm Hg) to give a brown syrup. Charged MTBE (22.7 L) andn-heptane (68.1 L), stirred at 25-30° C. for 5 h, filtered undernitrogen and washed with n-heptane (45.4 L, 2.0 volume) to give a secondcrop.

The two crops, 2-propanol (74.9 L) and n-heptane (74.9 L) were added toa glass-lined reactor and stirred under nitrogen atmosphere at 25-30° C.The above mass was heated to 75-80° C. and maintained at 75-80° C. for30 min. The mass was slowly cooled to 25-30° C. and maintained at 25-30°C. for 12 h. The solid was filtered, washed with 50% 2-propanol inn-heptane (68.1 L) and dried at 40-45° C. under vacuum (500-600 mm Hg)to give pure (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl 2-aminopropanoatehydrochloride as off white powder (11.54 kg, 62.2% yield). HPLC (Zorbax300 SCX, (250×4.6) mm, 5.0 μm; 55:45 [200 mm Phosphate buffer (pH:3):ACN], Flow: 2.0 mL/min) showed the product to be 94.0% pure.

Example 1o. (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl 2-aminopropanoatehydrochloride

A 25 mL flask equipped with a stir bar, temperature probe and nitrogeninlet was charged with(S,S)-1,1-bis(4-fluorophenyl)-1-hydroxypropan-2-yl2-((tert-butoxycarbonyl)amino)propanoate (3.0 g, 6.89 mmol) followed byCH₂Cl₂ (10 mL), and triethylsilane (4.4 mL, 27.56 mmol, 4 eq.). Theinternal temperature of the flask was maintained at 4° C. with anice-bath. Trifluoroacetic acid (10 mL, 130 mmol, 19 eq.) was added over15 minutes. The internal temperature did not exceed 8° C. during theaddition. The reaction was warmed to room temperature and stirred for 4hours. LC-MS indicated complete conversion to product. The solvent wasremoved under reduced pressure and co-evaporated with CH₂Cl₂ (3×20 mL).The resulting oil was dissolved in CH₂Cl₂ (50 mL), and added to asaturated solution of NaHCO₃ (100 mL) in small portions over 10 minutes.The aqueous layer was extracted with CH₂Cl₂ (25 mL), the combinedorganic layers were washed with brine and dried over Na₂SO₄ andconcentrated under reduced pressure. The oil was dissolved in MTBE (15mL), and 4N HCl in dioxane was added (1.8 mL) to give a whiteprecipitate. The solid was recrystallized from 2-propanol/heptane,collected by filtration, washed with heptane and dried in a vacuum ovenat 50° C. to give 1.85 g of the final compound in 75% yield.Spectroscopic data were identical to the compound isolated in Example1h.

Example 1p. (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl 2-aminopropanoatehydrochloride

In a 250 mL, three-neck round bottom flask, equipped with a magneticstir bar, a thermocouple and a nitrogen inlet, a mixture of MsOH (15.0mL, 230.0 mmol) and CH₂Cl₂ (15 mL) was cooled to 1° C.1,1,3,3-tetramethyldisiloxane (TMDS) (4.1 mL, 23.0 mmol) was added. Asolution of (S,S)-1,1-bis(4-fluorophenyl)-1-hydroxypropan-2-yl2-((tert-butoxycarbonyl)amino)propanoate (10.1 g, 23.0 mmol) in CH₂Cl₂(15 mL) was added slowly dropwise over the course of an hour to maintainan internal temperature below 3° C. After the addition was complete, thereaction mixture was stirred 45 min at which point the reaction wascomplete by HPLC analysis. An aqueous solution of sodium carbonate(saturated, 200 mL) was added slowly maintaining an internal temperaturebelow 20° C. The mixture was transferred to a separatory funnel. Thelayers were separated. The aqueous layer was extracted with CH₂Cl₂ (20mL×1). The combined organic layers were cloudy and washed with brine (20mL×1), dried over sodium sulfate and filtered to give an off-white goo.The crude material was taken up in MTBE (125 mL), and HCl (3 M in CPME,11.5 mL) was added with stirring. The white solids were collected andwashed with heptane (50 mL). The material was allowed to dry overnightin the fume hood. 8.03 g solids were collected (98% yield, 89% purity byHPLC with internal standard). ¹H NMR (400 MHz, CDCl₃) δ 8.64 (bs, 3H),7.21 (tdd, J=7.2, 5.1, 2.0 Hz, 4H), 6.98 (td, J=8.6, 6.2 Hz, 4H),5.77-5.59 (m, 1H), 4.05 (d, J=10.0 Hz, 1H), 3.96 (q, J=7.2 Hz, 1H), 1.23(d, J=6.1 Hz, 3H), 1.14 (d, J=7.2 Hz, 3H). ¹⁹F NMR (376 MHz, CDCl₃) δ−115.16, −115.52. ESIMS m/z 320.1 ([M+H]⁺).

Example 1q. (S)-1,1-bis(4-fluorophenyl)propan-2-ol

A 5 L flask was charged with (S)-1,1-bis(4-fluorophenyl)propane-1,2-diol(120 g, 431 mmol) and DCM (1200 mL). The flask was cooled to 0° C., andtriethylsilane (689 mL, 4314 mmol) was added followed by addition of TFA(332 mL, 4314 mmol). Addition took 12 minutes, and the temperature rosefrom −3° C. to −2° C. The mixture was stirred at 0° C. for 1 hour. After1 hr, the reaction mixture was neutralized with 4N NaOH (˜1.2 L), whilestill in the ice bath, to a pH of ˜10. The layers were separated and theaqueous phase was extracted with dichloromethane (1×). The combinedorganic extracts were dried over Na2SO4, filtered and concentrated invacuo to yield 159 g of a pale-yellow oil. The crude material was loadedonto a 1.5 kg ISCO silica column and eluted with an EtOAc/hexanegradient to afford 90.3 g of a white solid (83%). ¹H NMR (400 MHz,Chloroform-d) δ 7.35-7.28 (m, 2H), 7.25-7.18 (m, 2H), 7.05-6.93 (m, 4H),4.45 (m, 1H), 3.79 (d, J=8.3 Hz, 1H), 1.63 (d, J=3.7 Hz, 1H), 1.17 (d,J=6.1 Hz, 3H). ¹³C NMR (101 MHz, CDCl₃) δ 161.8 (d, J=245.7 Hz), 161.6(d, J=245.4 Hz), 138.2 (d, J=3.3 Hz), 137.0 (d, J=3.3 Hz), 130.2 (d,J=7.8 Hz), 129.6 (d, J=7.9 Hz), 115.7 (d, J=21.2 Hz), 115.5 (d, J=21.0Hz), 70.1, 58.6, 21.6. ¹⁹F NMR (376 MHz, CDCl3) δ −115.84, −116.16.ESIMS m/z 231.3 ([M-OH]+). Chiral HPLC analysis was performed using aChiralpak IA column (250×4.6 mm, P/N: 80325) with isocratic 85% hexanes(0.1% trifluoroacetic acid) and 15% isopropanol (0.1% trifluoroaceticacid) mobile phase (10 μL injected). Using a UV detector set to 265 nm,enantiomer #1 (major) eluted at 6.2 minutes and enantiomer #2 (minor)eluted at 6.8 minutes. The enantiopurity was determined to be 98% ee.

Example 1r. (S)-1,1-bis(4-fluorophenyl)propan-2-ol

A 50 mL, three-neck round bottom flask equipped with a magnetic stirrer,a thermocouple and a nitrogen inlet was charged with(S)-1,1-bis(4-fluorophenyl)propane-1,2-diol (1.0 g, 3.8 mmol), CH₂Cl₂ (3mL), and TMDS (2.0 mL, 1.1 mmol). TFA (5.8 mL, 7.6 mmol) was addeddropwise. After 30 min, the reaction was complete by HPLC analysis. Thereaction mixture was washed with a saturated aqueous solution of sodiumcarbonate (20 mL×2). The organic layer was dried over sodium sulfate,filtered and concentrated. The crude product was purified by columnchromatography (SiO₂, 0-40% EtOAc in hexanes) to give a colorless oil(0.68 g, 75% yield). ¹H NMR (400 MHz, CDCl₃) δ 7.38-7.29 (m, 2H),7.25-7.16 (m, 2H), 7.07-6.89 (m, 4H), 4.51-4.43 (m, 1H), 3.80 (d, J=8.2Hz, 1H), 1.53 (bs, 1H), 1.19 (d, J=6.1 Hz, 3H). ¹⁹F NMR (376 MHz, CDCl₃)δ −115.86, −116.20.

Example 1s. (S)-1,1-bis(4-fluorophenyl)propan-2-ol

A 100 mL, three-neck, round bottom flask equipped with a magneticstirrer, a thermocouple and a nitrogen inlet was charged with(S)-1,1-bis(4-fluorophenyl)propane-1,2-diol (1.23 g, 4.67 mmol), andCH₂Cl₂ (53 mL), and the resulting solution was cooled to 0° C. Neat PMHS(M_(N)=1700-3200, 2.9 g) was added followed by dropwise addition of neatTFA (5.4 g, 46.7 mmol). After 80 min, the reaction was quenched byaddition to 50 mL of 1 M NaOH. CH₂Cl₂ (30 mL) was added. The aqueouslayer was separated and extracted with additional CH₂Cl₂ (2×35 mL). Thecombined organics were washed with brine, dried (Na₂SO₄) and rotaryevaporated. The crude product was purified by column chromatography(SiO₂, 0-45% EtOAc in hexanes) to give a colorless oil (0.613 g, 53%yield). ¹H NMR (400 MHz, CDCl₃) δ 7.38-7.29 (m, 2H), 7.25-7.16 (m, 2H),7.07-6.89 (m, 4H), 4.51-4.43 (m, 1H), 3.80 (d, J=8.2 Hz, 1H), 1.53 (bs,1H), 1.19 (d, J=6.1 Hz, 3H). ¹⁹F NMR (376 MHz, CDCl₃) δ −115.86,−116.20. Chiral HPLC analysis showed a single enantiomer.

Example 1t. (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl2-((tert-butoxycarbonyl)amino)propanoate

A 250 mL flask equipped with a stir bar was charged with(S)-2-((tert-butoxycarbonyl)amino)propanoic acid (0.91 g, 4.8 mmol) andDCM (20 mL) and cooled to 0° C. Triethylamine (1.4 mL, 10 mmol) wasadded to the reaction flask. As pivaloyl chloride (0.59 mL, 4.8 mmol)was slowly added to the reaction mixture a white precipitate began toform. After stirring for 15 min at 0° C.,(S)-1,1-bis(4-fluorophenyl)propan-2-ol (993 mg, 4.0 mmol) was added,followed by N,N-dimethylpyridin-4-amine (49 mg, 0.4 mmol), and thereaction was stirred overnight at RT. The reaction was quenched withwater, and the layers were separated. The aqueous layer was extractedonce with DCM. The combined organic layers were dried with Na2SO4,filtered and concentrated to afford a colorless oil. The crude materialwas purified via silica gel chromatography by eluting with an ethylacetate/hexane gradient to afford the title compound as a white foam(1.4 g, 83%): ¹H NMR (300 MHz, CDCl₃) δ 7.29-7.17 (m, 4H), 7.03-6.92 (m,4H), 5.71 (dq, J=9.8, 6.2 Hz, 1H), 4.94 (d, J=8.0 Hz, 1H), 4.12 (q,J=7.1 Hz, 1H), 4.02 (d, J=9.9 Hz, 1H), 1.42 (s, 9H), 1.22 (d, J=6.2 Hz,3H), 0.84 (d, J=7.2 Hz, 3H); ¹³C NMR (126 MHz, CDCl₃) δ 172.8, 161.7 (d,J=246.1 Hz), 161.7 (d, J=245.6 Hz), 154.9, 137.0 (d, J=3.3 Hz), 136.8(d, J=3.4 Hz), 129.5 (d, J=7.9 Hz), 129.5 (d, J=7.8 Hz), 115.7 (d,J=21.3 Hz), 115.4 (d, J=21.3 Hz), 79.8, 72.9, 56.2, 49.2, 28.3, 19.2,18.1; ¹⁹F NMR (376 MHz, CDCl₃) δ −115.56, −115.97; ESIMS m/z 442.1([M+Na]⁺).

Example 1u. (S,S)-1,1-bis(4-fluorophenyl)propan-2-yl 2-aminopropanoatehydrochloride

A 3 L single-neck flask equipped with a stir bar was charged with(S,S)-1,1-bis(4-fluorophenyl)propan-2-yl2-((tert-butoxycarbonyl)amino)propanoate (130 g, 294 mmol) and dioxane(100 mL). HCl in dioxane (750 mL, 3 mol, 4M solution) was added to thestirring mixture at rtRT (20° C.). The reaction was stirred overnightand then concentrated in vacuo to yield a sticky, tan foam. Diethylether (1.75 L) was added and the heterogeneous mixture was vigorouslystirred for 30 min. The mixture was filtered, rinsed with diethyl ether,followed by hexane and vacuum dried to afford a white solid (104.7 g,100%): ¹H NMR (300 MHz, DMSO-d₆) δ 8.38 (s, 3H), 7.56-7.40 (m, 4H),7.18-7.10 (m, 4H), 5.77 (dq, J=12.2, 6.2 Hz, 1H), 4.27 (d, J=10.1 Hz,1H), 3.91 (q, J=7.1 Hz, 1H), 1.17 (d, J=6.1 Hz, 3H), 0.81 (d, J=7.2 Hz,3H); ¹³C NMR (101 MHz, DMSO-d₆) δ 169.5, 161.0 (d, J=243.2 Hz), 160.9(d, J=242.7 Hz), 137.8 (d, J=3.2 Hz), 137.3 (d, J=3.2 Hz), 130.0 (d,J=7.9 Hz), 129.8 (d, J=7.9 Hz), 115.4 (d, J=21.1 Hz), 115.2 (d, J=21.0Hz), 73.7, 54.7, 47.6, 18.8, 15.0; ¹⁹F NMR (376 MHz, DMSO-d₆) δ −115.89,−116.29; ESIMS m/z 320.1 ([M+H]⁺).

Example 1v. (S)-1,1-bis(4-fluorophenyl)propane-1,2-diol

A 5 L, 3-neck flask, equipped with overhead stirring, internaltemperature probe, addition funnel and nitrogen atmosphere, was chargedwith (4-fluorophenyl)magnesium bromide (1600 mL, 1600 mmol, 1M in THF).The mixture was cooled to 0° C. and a solution of (S)-ethyl lactate (60g, 483 mmol) in THF (500 ml) was slowly added via addition funnel (40min) and the temperature of the reaction never rose above 0° C. Whilestill cold (4° C.), the reaction was quenched with sat. aq. NH4Cl (250mL) and stirred until the reaction reached ambient temperature. Theliquid layer was decanted off from the white solid. The white solid wassuspended in EtOAc, filtered and rinsed with EtOAc. The combined organicphases were concentrated under vacuum. The residue was taken up inEtOAc, transferred to a separatory funnel, and washed with water. Theorganic phase was dried over Na2SO4, filtered and concentrated undervacuum to yield a yellow oil. The crude material was taken up inacetonitrile (500 mL) and extracted with hexane (2×300 mL). Theacetonitrile layer was dried over Na2SO4, filtered and concentrated toyield 117 g of a yellow oil. The crude material was chromatographed on a1.5 kg ISCO silica gel cartridge, eluting with an EtOAc/hexane gradientto afford 88.3 g of white solid (66%). ¹H NMR (400 MHz, Chloroform-d) δ7.59-7.49 (m, 2H), 7.41-7.32 (m, 2H), 7.07-6.92 (m, 4H), 4.74 (qd,J=6.2, 3.8 Hz, 1H), 3.00 (s, 1H), 1.81 (d, J=3.8 Hz, 1H), 1.08 (d, J=6.3Hz, 3H). 13C NMR (101 MHz, CDCl3) δ 161.9 (d, J=246.8 Hz), 161.7 (d,J=246.0 Hz), 141.2 (d, J=3.3 Hz), 139.6 (d, J=3.2 Hz), 128.1 (d, J=7.9Hz), 127.4 (d, J=8.0 Hz), 115.4 (d, J=21.3 Hz), 115.0 (d, J=21.3 Hz),79.3, 71.5, 16.9. ¹⁹F NMR (376 MHz, CDCl₃) δ −115.3, −115.9. ESIMS m/z263.1 ([M−H]−).

Example 1w. (S)-1,1-bis(4-fluorophenyl)propane-1,2-diol

Magnesium turnings (12.6 kg, 3.5 eq) and anhydrous tetrahydrofuran(115.6 L) were charged into a stainless steel reactor with stirringunder nitrogen atmosphere at 25-30° C. The reaction mixture was heatedto 40-45° C. A solution of 4-bromofluorobenzene in tetrahydrofuran(81.35 kg, 3.25 eq of 4-bromofluorobenzene in 115.6 L of THF) was addeddropwise at 50-55° C. and maintained for 30 min. The reaction mixturewas allowed to cool to 0-3° C., and then a solution of ethyl L-lactatein tetrahydrofuran (17.0 Kg, 1.0 eq of ethyl L-lactate in 84.2 L of THF)was added dropwise at 0-3° C. over a period of 2.0 h and maintained for30 min. A saturated solution of ammonium chloride (119.0 L, 41.65 kgammonium chloride in 119.0 L water) was added dropwise at 0-10° C. overa period of 2.0 h. The reaction mixture was filtered, and the solid waswashed with ethyl acetate (3×125.8 L). The filtrate was charged back tothe reactor and washed with brine solution (1×85.0 L, 5.0 vol). Theaqueous layer was re-extracted with ethyl acetate (1×125.8 L, 7.4volume), the combined organic layers were washed with brine (1×85.0 L,5.0 volume), dried over sodium sulphate (8.5 kg, 0.5 volume), filteredand concentrated completely at 40-45° C. under vacuum (500-600 mm Hg) togive a pale yellow oil. Hexanes (85.0 L, 5.0 volume) were added, andconcentrated below 45° C. under vacuum (500-600 mm Hg) until nodistillate was observed. Added hexanes (119.0 L), stirred for 15 min,cooled to 8-12° C. and maintained for 1 h. The solids were filtered andwashed with hexanes (1×17.0 L). The above wet solid was charged back tothe reactor, 2% MTBE in hexanes (119.0 L, 7.0 volume) were added andstirred at 25-30° C. for 30 min. Filtered the mass, washed with hexanes(51.0 L) and dried the solid at 35-40° C. under vacuum (500-600 mm Hg)to give (S)-1,1-bis(4-fluorophenyl)propane-1,2-diol as a pale yellowpowder (26.0 kg, 68.3% yield). HPLC (Hypersil BDS C18, (250×4.6) mm, 5.0μm; A: 0.1% TFA in water, B: ACN, Flow: 1.0 mL/min) showed the productto be 95.1% pure.

Example 1x. 3-(Acetyloxy)-4-methoxypicolinic acid

3-Hydroxy-4-methoxypicolinic acid (5.0 g, 29.6 mmol) was slurried in 50mL of pyridine and 50 mL of acetic anhydride at ambient temperature.After 1 h, a yellow solution had formed which was then stirredovernight. The solution was evaporated at 45° C. (2 mm Hg) to give 6.28g of tan solid (99% yield, mp=132-134° C.). ¹H NMR (400 MHz, DMSO-d₆) δ13.32 (s, 1H), 8.43 (d, J=5.5 Hz, 1H), 7.40 (d, J=5.5 Hz, 1H), 3.91 (s,3H), 2.27 (s, 3H). ¹³C NMR (101 MHz, DMSO-d₆) δ 167.95, 164.81, 158.34,147.87, 142.77, 136.18, 110.87, 56.59, 20.27. HRMS (m/z) calcd forC₉H₉NO₅ 211.0478, found 211.0481 ([M]⁺).

Example 1y. 3-(Acetyloxy)-4-methoxypicolinic acid

Pyridine (5.7 L, 1.0 volume), 3-hydroxy-4-methoxypicolinic acid (5.7 kg,1.0 eq) and acetic anhydride (15.73 L, 5.0 eq) were charged into aglass-lined reactor with stirring under nitrogen atmosphere at 25-30° C.The above reaction mass was stirred at 25-30° C. for 18 h. Aftercompletion of the reaction, 30% MTBE in hexanes (28.5 L, 5.0 volume,8.55 L MTBE in 19.95 L hexanes) was added, and the mixture was stirredat 25-30° C. for 2 h. The solid was filtered, washed with 20% MTBE inhexanes (34.2 L, 6.0 volume, 6.8 L MTBE in 27.4 L hexanes) and allowedto dry. The solid was dried at 25-30° C. under vacuum (500-600 mm Hg) togive 3-(acetyloxy)-4-methoxypicolinic acid as a pale yellow powder (6.85kg, 96.3% yield). HPLC (Zorbax SB-Aq, (250×4.6) mm, 5.0 μm; A: 0.1% TFAin water, B: Acetonitrile, Flow: 1.0 mL/min) showed the product to be98.5% pure.

Example 1z. (S,S)-1,1-bis(4-fluorophenyl)-propan-2-yl2-(3-acetoxy-4-methoxypicolinamido)propanoate

A flask equipped with a stir bar and nitrogen inlet was charged with3-acetoxy-4-methoxypicolinic acid (2.97 g, 14.05 mmol) and DCM (28.1mL). DIPEA (9.82 mL, 56.2 mmol) was added and the reaction was cooled to−15° C. Methanesulfonyl chloride (1.095 mL, 14.05 mmol) was then slowlyadded. After stirring for 15 minutes,(S)-1,1-bis(4-fluorophenyl)propan-2-yl L-alaninate hydrochloride (5 g,14.05 mmol) was added. After 90 minutes of stirring, the mixture wasallowed to warm. The solution was poured into saturated NH₄Cl (aq) in aseparatory funnel. The layers were separated, and the organic layer waswashed with 1:1 brine/1N HCl then with water. The DCM layer was driedover Na₂SO₄, filtered and concentrated to provide an oil. The crudematerial was purified via silica gel chromatography by eluting with anethyl acetate/hexane gradient to afford the title compound as a whitefoam (2.9 g, 38% yield): ¹H NMR (400 MHz, CDCl₃) δ 8.39 (s, 1H), 8.32(d, J=5.4 Hz, 1H), 7.26-7.16 (m, 4H), 7.03-6.87 (m, 5H), 5.71 (dq,J=9.6, 6.1 Hz, 1H), 4.55 (dd, J=8.0, 7.1 Hz, 1H), 4.04 (d, J=9.6 Hz,1H), 3.91 (s, 3H), 2.38 (s, 3H), 1.22 (d, J=6.1 Hz, 3H), 0.99 (d, J=7.2Hz, 3H); ¹⁹F NMR (376 MHz, CDCl₃) δ −115.61, −115.96; HRMS-ESI (m/z)[M+H]⁺ calcd for C₂₇H₂₇F₂N₂O₆, 512.1759; found, 513.1825.

What is claimed is:
 1. A process for the preparation of the compound ofFormula C

wherein X is Cl, Br, HSO₄, H₂PO₄ or CH₃SO₃; which comprises thefollowing steps: a) creating a first mixture containing the compound ofFormula G,

an acylating agent and a base; b) adding the compound of Formula H

to the first mixture to form a second mixture; c) isolating the compoundof Formula I

from the second mixture; d) creating a third mixture containing thecompound of Formula I, an acid and a reducing agent; e) isolating thecompound of Formula J from the third mixture;

f) creating a fourth mixture containing the compound of Formula J and astrong acid; wherein the strong is HCl, HBr, H₂SO₄, H₃PO₄ or CH₃SO₃H;and g) isolating the compound of Formula C from the fourth mixture. 2.The process of claim 1 wherein the acylating agent is an acid chlorideof the Formula RCOCl, wherein R is a C₁-C₄ alkyl.
 3. The process ofclaim 1 wherein the first mixture further comprises a solvent selectedfrom the group including, DCM, DCE, ACN, isopropyl acetate, THF,2-MeTHF, and mixtures thereof.
 4. The process of claim 1 wherein thebase may be selected from the group including TEA, DIPEA, pyridine, andmixtures thereof.
 5. The process of claim 1 further comprising theaddition of DMAP (4-(dimethylamino)pyridine) to the first mixture. 6.The process of claim 1 wherein the acid in the third mixture istrifluoroacetic acid or methanesulfonic acid.
 7. The process of claim 1wherein the reducing agent is selected from the group including sodiumborohydride, sodium triacetoxyborohydride, and an organosilicon hydride.8. The process of claim 7 wherein the organosilicon hydride is selectedfrom the group including triethylsilane, poly(methylhydrosiloxane) and1,1,3,3-tetramethyldisiloxane.
 9. The process of claim 1 wherein thefourth mixture is maintained under anhydrous conditions.
 10. A processfor the preparation of the compound of Formula C

wherein X is Cl, Br, HSO₄, H₂PO₄ or CH₃SO₃; which comprises thefollowing steps: a) creating a first mixture containing the compound ofFormula H

a reducing agent and an acid; b) isolating the compound of Formula Kfrom the first mixture;

c) creating a second mixture containing the compound of Formula G,

an acylating agent and a base; f) adding the compound of Formula K tothe second mixture to form a third mixture; g) isolating the compound ofFormula L from the third mixture;

h) creating a fourth mixture containing the compound of Formula L and astrong acid; wherein the strong acid is HCl, HBr, H₂SO₄, H₃PO₄ orCH₃SO₃H; and i) isolating the compound of Formula C from the fourthmixture.
 11. The process of claim 10 wherein the acid in the firstmixture is trifluoroacetic acid or methanesulfonic acid.
 12. The processof claim 10 wherein the reducing agent is selected from the groupincluding sodium borohydride, sodium triacetoxyborohydride, and anorganosilicon hydride.
 13. The process of claim 12 wherein theorganosilicon hydride is selected from the group includingtriethylsilane, poly(methylhydrosiloxane) and1,1,3,3-tetramethyldisiloxane.
 14. The process of claim 10 wherein theacylating agent is an acid chloride of the Formula RCOCl, wherein R is aC₁-C₄ alkyl.
 15. The process of claim 10 wherein the second mixturefurther comprises a solvent selected from the group including, DCM, DCE,ACN, isopropyl acetate, THF, 2-MeTHF, and mixtures thereof.
 16. Theprocess of claim 9 wherein the base in the second mixture may beselected from the group including TEA, DIPEA, pyridine, and mixturesthereof.
 17. The process of claim 10 further comprising the addition ofDMAP (4-(dimethylamino)pyridine) to the second mixture.
 18. The processof claim 10 wherein the fourth mixture is maintained under anhydrousconditions.